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I have CF, but it will never have me!

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, August 11, 2015. Ever heard the old expression, "Life is an open book"? Like a book, life has a beginning, a middle and an end. I guess in short, everyone dies but not...

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I have CF, but it will never have me! | thedriveat35.blogspot.com Reviews

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I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, August 11, 2015. Ever heard the old expression, Life is an open book? Like a book, life has a beginning, a middle and an end. I guess in short, everyone dies but not...

<META> KEYWORDS

1 life and death

2 heck no

3 perhaps it's perspective

4 posted by

5 andy lipman

6 no comments

7 labels book

8 cystic fibrosis

9 life

10 changes

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life and death,heck no,perhaps it's perspective,posted by,andy lipman,no comments,labels book,cystic fibrosis,life,changes,quack,play ball,andy,howard at 39,saved my life,love you howard,your best friend,1 comment,what's the point,2 comments,foster care

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I have CF, but it will never have me! | thedriveat35.blogspot.com Reviews

https://thedriveat35.blogspot.com

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, August 11, 2015. Ever heard the old expression, "Life is an open book"? Like a book, life has a beginning, a middle and an end. I guess in short, everyone dies but not...

INTERNAL PAGES

thedriveat35.blogspot.com

1

I have CF, but it will never have me!: November 2014

http://thedriveat35.blogspot.com/2014_11_01_archive.html

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, November 11, 2014. And the winter is. First off, that was a movie. Second of all, it takes a far longer time to defeat a resilient adversary than two hours. What peopl...

2

I have CF, but it will never have me!: January 2015

http://thedriveat35.blogspot.com/2015_01_01_archive.html

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, January 13, 2015. A few months into my run with Fluffy En Fuego, one of our players, Bob Foster, told us that he needed our help.again. "Again? All my best,.

3

I have CF, but it will never have me!: April 2014

http://thedriveat35.blogspot.com/2014_04_01_archive.html

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Thursday, April 3, 2014. One Heck of a March! The journey on IV therapy officially began the morning of Wednesday February 26th when my PICC line was inserted at Emory hospital.

4

I have CF, but it will never have me!: Life & Death

http://thedriveat35.blogspot.com/2015/08/life-death-i-remember-few-years-ago.html

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, August 11, 2015. Ever heard the old expression, "Life is an open book"? Like a book, life has a beginning, a middle and an end. I guess in short, everyone dies but not...

5

I have CF, but it will never have me!: Changes

http://thedriveat35.blogspot.com/2015/05/changes.html

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Wednesday, May 20, 2015. So it's been a crazy few weeks for me and my family. Mary, I get it. More great news for the CF Community. The girls' softball team I coached made it a...

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toi-marie.blogspot.com

I'm Just Sayin'...: December 2010

http://toi-marie.blogspot.com/2010_12_01_archive.html

Black or White, Right or Wrong. Thoughts, stories, rants and messages from a judicious perspective. Wednesday, December 15, 2010. It's "that" time of year! We are, as a family, doing our best to making lasting, loving memories with our children and grandchildren. So where does meanness factor in and how do you explain it to children? Don't be a scrooge.Enjoy the Holidaze! Subscribe to: Posts (Atom). Its that time of year! Most photos courtesy of www.weheartit.com. I have CF, but it will never have me!

cfjourney.wordpress.com

LISTED | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/2012/03/06/listed

My Journey with Cystic Fibrosis. One day at a time . . . March 6, 2012. It’s official…. As of 3pm today, 3-6-12, I have been listed for double lung transplant. Started ivs yesterday. Just short of 2 weeks after finishing my last ivs. Thus is how it will be until the surgery. It’s wierd waiting for some innocent person that was generous enough to sign up as a donor, to pass on. That will be my first goal! Running… Seems so simple, but I haven’t been able to in many years…. Here we go again…. Please read M...

cfjourney.wordpress.com

Part IV | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/part-iv

My Journey with Cystic Fibrosis. One day at a time . . . I need to first apologize to my followers… I know it seems like I dropped off the planet. I recently read some of my last posts and I’m so glad I wrote those. It makes me appreciate where I am today. I did not die! I am no longer suffering! I received my Double Lung Transplant on June 6, 2012! I was told I would not be able to leave the hospital until new lungs came in. Very scary! I was scheduled for surgery on June 6th at 2am. My leg muscles were...

cfjourney.wordpress.com

Feeling Awesome !!! | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/2014/04/29/feeling-awesome

My Journey with Cystic Fibrosis. One day at a time . . . April 29, 2014. I can’t believe how I just abandoned this blog since transplant. The first year was a slow recovery and dealt with depression. Then I tried to activate the 2 step authorization on wordpress and it totally messed me up and I couldnt get in! I finally contacted support and got the whole thing deactivated. So, here I am, almost 2 years post transplant and I’m feeling amazing! I hope to keep up with my posts. We shall see. I added a Par...

cfjourney.wordpress.com

Just Reminiscing | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/2013/05/25/just-reminiscing

My Journey with Cystic Fibrosis. One day at a time . . . May 25, 2013. I wish I could go and talk to myself pre transplant and tell myself that its going to be ok… you will breath like a normal person… you need the transplant or your life WILL end. I’m enjoying life… I have an 18 year old that drives me crazy. And it’s all good. My donor, Bernadette, saved my life and I am forever grateful. I added a Part IV above! Leave a Reply Cancel reply. Enter your comment here. Address never made public). Eva &#821...

cfjourney.wordpress.com

Because I Don’t Ever Want to Forget… | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/2012/04/17/because-i-dont-ever-want-to-forget

My Journey with Cystic Fibrosis. One day at a time . . . Because I Don’t Ever Want to Forget…. April 17, 2012. As I wait for my call for transplant, it occurred to me that I will be entering a brand new world. I don’t ever want to forget where I came from. I fought to get to this point and in my “new” existence, I don’t ever want to give up either. By reminding myself of my struggles, it should help me fight…. So, here goes… Don’t ever forget…. The enormous amount of mucus I coughed up. The limit on my s...

cfjourney.wordpress.com

As time passes … | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/2012/05/25/as-time-passes

My Journey with Cystic Fibrosis. One day at a time . . . As time passes …. May 25, 2012. I know it’s been a while since my last post. It’s been rough. I’ve been on and off IVs and am now on the worst one ever, the polymyxin. Started it Wednesday night after a little over a week on another IV med. When I got to the hospital I actually had to wait for a bed! Lungs can’t stay out of the body for very long! I thought – this must mean it’s a go! I was the primary for the lungs! I can’t wait to take a de...

cfjourney.wordpress.com

My Story-Part I | My Journey with Cystic Fibrosis

https://cfjourney.wordpress.com/my-story

My Journey with Cystic Fibrosis. One day at a time . . . Ok… So i’ll attempt to share my story the best I can…. I was born in 1967, a healthy baby girl. No medical problems, lived a normal childhood. When I was in 3rd grade, I had my first pneumonia, missed one month of school, and recovered. When I was in 6th grade, I had my 2nd pneumonia, and again recovered. When I was in 9th grade, my 3rd pneumonia, suspicion began. I felt much better after this and all was fine. Gave me a load of pills, but never ga...

toi-marie.blogspot.com

I'm Just Sayin'...: November 2010

http://toi-marie.blogspot.com/2010_11_01_archive.html

Black or White, Right or Wrong. Thoughts, stories, rants and messages from a judicious perspective. Tuesday, November 2, 2010. The Day Before Tomorrow. As I sat in my chair, laptop in front of me, and contemplated writing this blog, the sun peaked through the clouds casting a bright light on my screen with warmth surrounding me. A sign? Is the anticipation of an upcoming event more traumatic and/or more exciting than that of the actual event? Taken the time to appreciate the today we were given? Taken th...

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thedriveat35.blogspot.com

I have CF, but it will never have me!

I have CF, but it will never have me! This is a blog that Andy has written to describe his battle with cystic fibrosis. Andy is 40 years old and is married to his beautiful bride Andrea and has two miracle children, Avery and Ethan. Andy appreciates each day and hopes to show the doubters that in his world CF stands for Can Fight! Tuesday, August 11, 2015. Ever heard the old expression, "Life is an open book"? Like a book, life has a beginning, a middle and an end. I guess in short, everyone dies but not...

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